Kleijer WJ - Search Results

1

First trimester diagnosis of Hunter syndrome on chorionic villi.

Kleijer WJ, van Diggelen OP, Janse HC, Galjaard H, Dumez Y, Boué J. Kleijer WJ, et al. Lancet. 1984 Aug 25;2(8400):472. doi: 10.1016/s0140-6736(84)92952-0. Lancet. 1984. PMID: 6147543 No abstract available.

2

First-trimester diagnosis of galactosaemia.

Kleijer WJ, Janse HC, van Diggelen OP, Macek M, Hajek Z, Gillett MG, Holton JB. Kleijer WJ, et al. Lancet. 1986 Mar 29;1(8483):748. doi: 10.1016/s0140-6736(86)91149-9. Lancet. 1986. PMID: 2870264 No abstract available.

3

First-trimester diagnosis of mucopolysaccharidosis IIIA (Sanfilippo A disease).

Kleijer WJ, Janse HC, Vosters RP, Niermeijer MF, van de Kamp JJ. Kleijer WJ, et al. N Engl J Med. 1986 Jan 16;314(3):185-6. doi: 10.1056/NEJM198601163140319. N Engl J Med. 1986. PMID: 3079882 No abstract available.

4

First trimester diagnosis of Wolman's disease.

van Diggelen OP, von Koskull H, Ammälä P, Vredeveldt GT, Janse HC, Kleijer WJ. van Diggelen OP, et al. Among authors: kleijer wj. Prenat Diagn. 1988 Nov;8(9):661-3. doi: 10.1002/pd.1970080905. Prenat Diagn. 1988. PMID: 3211854

5

First-trimester diagnosis of maple syrup urine disease on intact chorionic villi.

Kleijer WJ, Horsman D, Mancini GM, Fois A, Boue J. Kleijer WJ, et al. N Engl J Med. 1985 Dec 19;313(25):1608. doi: 10.1056/nejm198512193132514. N Engl J Med. 1985. PMID: 4069174 No abstract available.

6

Disaccharidases in amniotic fluid as possible prenatal marker for cystic fibrosis.

van Diggelen OP, Janse HC, Kleijer WJ. van Diggelen OP, et al. Among authors: kleijer wj. Lancet. 1983 Apr 9;1(8328):817. doi: 10.1016/s0140-6736(83)91869-x. Lancet. 1983. PMID: 6132147 No abstract available.

7

First-trimester (chorion biopsy) diagnosis of citrullinaemia and methylmalonicaciduria.

Kleijer WJ, Thoomes R, Galjaard H, Wendel U, Fowler B. Kleijer WJ, et al. Lancet. 1984 Dec 8;2(8415):1340. doi: 10.1016/s0140-6736(84)90848-1. Lancet. 1984. PMID: 6150349 No abstract available.

8

First-trimester diagnosis of Krabbe's disease by direct enzyme analysis of chorionic villi.

Kleijer WJ, Mancini GM, Jahoda MG, Vosters RP, Sachs ES, Niermeijer MF, Galjaard H. Kleijer WJ, et al. N Engl J Med. 1984 Nov 8;311(19):1257. N Engl J Med. 1984. PMID: 6493280 No abstract available.

9

Lysosomal alpha-N-acetylgalactosaminidase deficiency: a new inherited metabolic disease.

van Diggelen OP, Schindler D, Kleijer WJ, Huijmans JM, Galjaard H, Linden HU, Peter-Katalinic J, Egge H, Dabrowski U, Cantz M. van Diggelen OP, et al. Among authors: kleijer wj. Lancet. 1987 Oct 3;2(8562):804. doi: 10.1016/s0140-6736(87)92542-6. Lancet. 1987. PMID: 2889023 No abstract available.

10

[Initial experiences with the prenatal diagnosis of congenital disorders in the 8th-9th pregnancy week by analysis of the chorionic villi].

Jahoda M, Sachs ES, Kleijer WJ, Drogendijk AC, Galjaard H. Jahoda M, et al. Among authors: kleijer wj. Ned Tijdschr Geneeskd. 1984 Mar 10;128(10):436-42. Ned Tijdschr Geneeskd. 1984. PMID: 6709079 Dutch. No abstract available.

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